Development of an Oral Immunotherapy-Related Parental Burden Scale

Author:

Maeta Akihiro,Takaoka Yuri,Hamada Masaaki,Nakano Atsuko,Sumimoto Shinichi,Anzai Kaori,Tanaka Yukiko,Morikawa Satoru,Kameda Makoto,Takahashi Kyoko

Abstract

Introduction: Oral immunotherapy (OIT) imposes a burden on parents and their children with food allergies (FAs). We already developed a questionnaire for OIT-related Parental Burden (OIT-PB) scale. However, the previous questionnaire had some problems. This study modified OIT-PB and verified its reliability and validity. Methods: A 20-item draft covering the physical and mental burdens caused by OIT was prepared jointly with multiple allergists. The Food Allergy Quality of Life Questionnaire-Parental Burden (FAQLQ-PB) and Stress Response Scale-18 (SRS-18) were used to verify concurrent validity. A questionnaire survey was administered during treatment to parents of FA children who had started OIT for the first time. An additional OIT-PB survey was performed at one specific institution 1 week after the posttreatment survey. Results: The responses of 64 of the 76 recruited parents were analyzed. Of the 20 questions, 1 item was excluded owing to the floor effect, 1 was excluded because its commonality was less than 0.2, and 2 were excluded because their factor loading values were less than 0.4. Factor analysis was used to classify the OIT-PB into the following 4 subscales: “burden caused by adherence to treatment plan,” “anxiety about symptom-induced risk,” “burden due to patient’s eating behavior,” and “anxiety about treatment effect.” The Cronbach’s α for all 16 items of the OIT-PB was 0.893; Cronbach’s α for each subscale was 0.876, 0.898, 0.874, and 0.717. The re-test reliability coefficient was 0.864 (95% confidence interval [CI]: 0.720−0.937, p < 0.001). A significant positive correlation was found between the OIT-PB and FAQLQ-PB (R = 0.610 [95% CI: 0.422−0.747], p < 0.001) and the SRS-18 (R = 0.522 [95% CI: 0.306–0.687], p < 0.001). A significant negative correlation was found between the rate of increase in OIT food intake and the “anxiety about treatment effect” score (R = −0.355 [95% CI: −0.558–0.112], p < 0.001). Parents of children on the hen’s egg OIT treatment scored higher on the “burden due to patient’s eating behavior” subscale than did parents of children on the milk and wheat OIT treatment. Conclusion: The burden of OIT experienced by parents can be broadly classified into four categories. The modified OIT-PB was able to evaluate them individually and was shown to have reliability and validity. This scale is expected to be useful in the development of OIT that considers not only therapeutic effect but also the burden experienced by FA children and their parents.

Publisher

S. Karger AG

Subject

Immunology,General Medicine,Immunology and Allergy

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